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首页> 外文期刊>Applied Nanoscience >Dispersed gold nanoparticles potentially ruin gold barley yellow dwarf virus and eliminate virus infectivity hazards
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Dispersed gold nanoparticles potentially ruin gold barley yellow dwarf virus and eliminate virus infectivity hazards

机译:分散的金纳米粒子可能破坏金大麦黄矮病毒并消除病毒感染性危害

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Gold nanoparticles (AuNPs) application melted barley yellow dwarf virus-PAV (BYDV-PAV) spherical nanoparticle capsids. Synergistic therapeutic effects for plant virus resistance were induced by interaction with binding units of prepared AuNPs in a water solution which was characterized and evaluated by zeta sizer, zeta potential and transmission electron microscopy (TEM). The yield of purified nanoparticles of BYDV-PAV was obtained from Hordeum vulgare (Barley) cultivars, local and Giza 121/Justo. It was 0.62?mg/ml from 27.30?g of infected leaves at an A260/A280 ratio. Virus nanoparticle has a spherical shape 30?nm in size by TEM. BYDV-PAV combined with AuNPs to challenge virus function in vivo and in vitro. Dual AuNPs existence in vivo and in vitro affected compacted configuration of viral capsid protein in the interior surface of capsomers, the outer surface, or between the interface of coat protein subunits for 24 and 48?h incubation period in vitro at room temperature. The sizes of AuNPs that had a potentially dramatic deteriorated effect are 3.151 and 31.67?nm with a different intensity of 75.3% for the former and 24.7% for the latter, which enhances optical sensing applications to eliminate virus infectivity. Damages of capsid protein due to AuNPs on the surface of virus subunits caused variable performance in four different types of TEM named puffed, deteriorated and decorated, ruined and vanished. Viral yield showed remarkably high-intensity degree of particle symmetry and uniformity in the local cultivar greater than in Giza 121/Justo cultivar. A high yield of ruined VLPs in the local cultivar than Justo cultivar was noticed. AuNPs indicated complete lysed VLPs and some deteriorated VLPs at 48?h.
机译:金纳米颗粒(AuNPs)应用熔化了大麦黄矮病毒-PAV(BYDV-PAV)球形纳米颗粒衣壳。通过与制备的AuNPs的结合单元在水溶液中的相互作用,诱导了对植物病毒抗性的协同治疗作用,并通过zeta大小测定仪,zeta电势和透射电子显微镜(TEM)对其进行了表征和评估。 BYDV-PAV的纯化纳米颗粒的产量是从大麦,本地和吉萨121 / Justo品种获得的。从27.30μg的受感染叶片以A260 / A280的比率为0.62μg/ ml。通过TEM,病毒纳米颗粒具有30?nm的球形形状。 BYDV-PAV与AuNPs结合可在体内和体外挑战病毒功能。在室温下体外培养24和48小时后,体内和体外双重AuNP的存在会影响衣壳蛋白内表面,外表面或外壳蛋白亚基界面之间的病毒衣壳蛋白的紧密构型。具有潜在的显着恶化效果的AuNP的大小分别为3.151和31.67?nm,前者的强度分别为75.3%,后者的强度为24.7%,这增强了光学传感应用以消除病毒的感染性。病毒亚基表面上的AuNPs引起的衣壳蛋白损伤在四种不同类型的TEM中表现出变化的性能,分别称为膨化,变质和修饰,破坏和消失。与吉萨121 / Justo品种相比,本地品种的病毒产量表现出明显更高的颗粒对称性和均匀性。注意到本地品种的VLP破坏产量比Justo品种高。 AuNPs在48?h时显示完全裂解的VLP和一些劣化的VLP。

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